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首页> 外文期刊>Journal of the American Chemical Society >Highly Stereospecific Cross-Coupling Reactions of Anomeric Stannanes for the Synthesis of C-Aryl Glycosides
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Highly Stereospecific Cross-Coupling Reactions of Anomeric Stannanes for the Synthesis of C-Aryl Glycosides

机译:端粒锡烷的高度立体特异性交叉偶联反应,用于合成C-芳基糖苷

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摘要

We demonstrate that configurationally stable anomeric stannanes undergo a stereospecific cross-coupling reaction with aromatic halides in the presence of a palladium catalyst with exceptionally high levels of stereocontrol. In addition to a broad substrate scope (>40 examples), this reaction eliminates critical problems inherent to nucleophilic displacement methods and is applicable to (hetero)aromatics, peptides, pharmaceuticals, common monosaccharides, and saccharides containing free hydroxyl groups.
机译:我们证明,在钯催化剂存在下,立体稳定的异头锡烷与芳族卤化物进行立体有规的交叉偶联反应。除了广泛的底物范围(> 40个实例)之外,该反应消除了亲核取代方法固有的关键问题,适用于(杂)芳族化合物,肽,药物,常见的单糖和含有游离羟基的糖。

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  • 来源
    《Journal of the American Chemical Society》 |2016年第37期|12049-12052|共4页
  • 作者单位

    Department of Chemistry and Biochemistry, University of Colorado, Boulder, Colorado 80309, United States;

    Department of Chemistry and Biochemistry, University of Colorado, Boulder, Colorado 80309, United States;

    Department of Chemistry and Biochemistry, University of Colorado, Boulder, Colorado 80309, United States;

    Department of Chemistry and Biochemistry, University of Colorado, Boulder, Colorado 80309, United States;

    Department of Chemistry and Biochemistry, University of Colorado, Boulder, Colorado 80309, United States;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
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